ClinicalTrials.Veeva

Menu

Iron Absorption From GDS Capsules

F

Federal Institute of Technology (ETH) Zurich

Status

Completed

Conditions

Iron Deficiency

Treatments

Dietary Supplement: control, meal
Dietary Supplement: control, no meal
Dietary Supplement: GDS, no meal
Dietary Supplement: GDS, meal

Study type

Interventional

Funder types

Other

Identifiers

NCT01874496
EK 2013-N-05

Details and patient eligibility

About

Slow release iron capsules have been designed based on the gastric delivery system. Iron absorption from those capsules administered with and without meals will be measured using stable iron isotopes.

Enrollment

4 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • female,
  • age 18-50 years,
  • max. body weight 65 kg,
  • serum ferritin < 35µg/l

Exclusion criteria

  • pregnancy,
  • lactation,
  • regular intake of medication,
  • blood donation or significant blood losses over the past 4 months

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

4 participants in 4 patient groups

GDS, meal
Experimental group
Description:
GDS, meal
Treatment:
Dietary Supplement: GDS, meal
GDS, no meal
Experimental group
Description:
GDS, no meal
Treatment:
Dietary Supplement: GDS, no meal
control, no meal
Active Comparator group
Description:
control, no meal
Treatment:
Dietary Supplement: control, no meal
control, meal
Active Comparator group
Description:
control, meal
Treatment:
Dietary Supplement: control, meal

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems